WO2009048917A2 - Hydrolyse de fibres augmentée par addition de protéase - Google Patents

Hydrolyse de fibres augmentée par addition de protéase Download PDF

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Publication number
WO2009048917A2
WO2009048917A2 PCT/US2008/079152 US2008079152W WO2009048917A2 WO 2009048917 A2 WO2009048917 A2 WO 2009048917A2 US 2008079152 W US2008079152 W US 2008079152W WO 2009048917 A2 WO2009048917 A2 WO 2009048917A2
Authority
WO
WIPO (PCT)
Prior art keywords
protease
seq
fiber
glucose
fiber feedstock
Prior art date
Application number
PCT/US2008/079152
Other languages
English (en)
Other versions
WO2009048917A3 (fr
Inventor
Charles A. Abbas
Wu-Li Bao
Original Assignee
Archer-Daniels-Midland Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Archer-Daniels-Midland Company filed Critical Archer-Daniels-Midland Company
Priority to EP08836912.9A priority Critical patent/EP2201127B1/fr
Priority to CA2702279A priority patent/CA2702279C/fr
Priority to BRPI0816621A priority patent/BRPI0816621A2/pt
Priority to ES08836912.9T priority patent/ES2538995T3/es
Publication of WO2009048917A2 publication Critical patent/WO2009048917A2/fr
Publication of WO2009048917A3 publication Critical patent/WO2009048917A3/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00—Preparation of compounds containing saccharide radicals
    • C12P19/02—Monosaccharides
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00—Preparation of compounds containing saccharide radicals
    • C12P19/20—Preparation of compounds containing saccharide radicals produced by the action of an exo-1,4 alpha-glucosidase, e.g. dextrose
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00—Technologies for the production of fuel of non-fossil origin
    • Y02E50/10—Biofuels, e.g. bio-diesel

Definitions

  • Embodiments relate to, but are not limited to, the field of agricultural product production. Embodiments relate, for example, to methods for increasing the free glucose and other organic matter available from a fiber feedstock for fermentation and other applications.
  • a large quantity and variety of fiber feedstocks are available from agricultural processing operations. These fiber feedstocks (also called cellulosic feedstocks, biomass, or lignocellulosics) may be used, for example, to produce fuel, to produce industrial chemicals, or as other value-added food and feed products.
  • a cellulosic feedstock is largely comprised of plant cell walls with cellulose, hemicellulose, lignin, and protein polymers as the primary constituents.
  • the hydrolysis or breakdown of these feedstocks uses singly or a combination of enzymatic and thermochemical methods that result in the production of monomers and oligomers of carbohydrates.
  • the hydrolyzed mix can serve as feedstocks to produce fuel, chemicals, and other products. Similar hydrolysis schemes are employed with most plant fibers that facilitate the release of glucose and other carbohydrates from fiber feedstocks.
  • Embodiments of the invention are typically directed to providing a method for increasing the amount of glucose and other carbohydrates obtained from hydrolysis of a low- starch or no- starch fiber stream by hydrolyzing the fiber stream in the presence of protease and one or more of cellulase and hemicellulase.
  • Embodiments include a method for increasing the amount of glucose and other organic matter released from a fiber feedstock, comprising reacting a fiber feedstock with a mixture of reactants comprising at least one protease and at least one member of the group consisting of cellulase and hemicellulase; and obtaining a reaction product from the fiber feedstock and the mixture of reactants comprising glucose.
  • the amount of glucose in the reaction product (measured as a percentage of the fiber feedstock mass) is greater than the amount of glucose obtained from reaction of the fiber feedstock under the same conditions as the reaction including protease, but with at least one member selected from the group consisting of cellulase and hemicellulase and excluding protease.
  • the mixture of reactants used to increase the amount of glucose and other organic matter released from the fiber stream does not include amylases.
  • Proteases are enzymes that have found a great number of uses in the industrial production of detergents, animal hide processing, meat tenderizing as well as in other food applications involving animal and plant materials. As a group they represent one of the largest classes of hydrolytic enzymes which posses a wide range of specificities towards amino acid sequences, different pH and temperature optima, and different amino acids at active sites with some (i.e. metallo-proteases) requiring cations such as zinc or iron for optimal activity.
  • metallo-proteases requiring cations such as zinc or iron for optimal activity.
  • a variety of proteases may be suitable for use in embodiments of the invention, typically an acid fungal protease is preferred.
  • the acid fungal protease has an amino acid sequence at least 95% identical to the amino acid sequence of SEQ ID NO: 1.
  • the protease is selected from the group consisting of Aspergillus saitoi aspartic protease, or aspartic proteases from molds that are members of the genera of the Ascomycetous fungi represented by the genera Aspergillus, Mucor, Rhizopus, and Penicillium.
  • the protease is Aspergillus saitoi aspartic protease, which has the amino acid sequence of SEQ ID NO: 1.
  • Fiber feedstocks are suitable for use in embodiments of the invention.
  • Fiber feedstocks include, but are not limited to, corn stover, corn gluten feed (CGF), distillers' dried grains (DDG), distillers' dried grains with solubles (DDGS), switchgrass, miscanthus, soyhulls, wheat chaff, and wheat straw.
  • CGF corn gluten feed
  • DDG distillers' dried grains
  • DDGS distillers' dried grains with solubles
  • switchgrass miscanthus
  • soyhulls soyhulls
  • wheat chaff and wheat straw.
  • the fiber feedstock includes less than 20% starch by weight, less than 10% starch by weight, less than 5% starch by weight, or less than 1% starch by weight.
  • the fiber feedstock includes no starch.
  • a number of cellulases are suitable for use in typical embodiments of the invention. These include, for example, but are not limited to CELLUCLAST® (a Novozyme product), which is a l,4-(l,3:l,4)- ⁇ -D-Glucan 4-glucano-hydrolase produced by submerged fermentation of the fungus Trichoderma reesei, deposited as ATCC No. 26921; or GC-220 (a Genencor product).
  • CELLUCLAST® Novozyme product
  • Other useful cellulases include those from T. reesei, other species of Trichoderma, species of Aspergillus, species of Crysosporium, species of Clostridium or cellulases from other bacterial and fungal species.
  • a variety of hemicellulases are suitable for use in typical embodiments of the invention, including, for example, but not limited to Ultraflo L (Novozyme), Multifect Xylanase (Genencor), Viscozyme L (Novozyme), and Viscostar L (Dyadic).
  • the reaction products may also include one or more of arabinose, xylose, galactose, mannose, cellobiose, xylobiose ,acetyl groups, phytosterols, phenolic compounds and oligomers of these compounds.
  • the amount of glucose in the reaction product (measured as a percentage of the fiber feedstock mass) following protease addition is greater than the amount of glucose obtained from reaction of the fiber feedstock without protease by at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or at least 100%.
  • a further embodiment includes a method for obtaining a solid residue from the enzyme treated fiber for the production of biooil, comprising preparing a glucose-enriched fiber feedstock reaction product as described in other embodiments of the invention, and separating said reaction product into a solid hydrolyzed fiber fraction and a liquid fraction. This solid fraction may then be used as a fuel for biooil production.
  • the process employed in the above treatment is often referred to as hydrotreating, or HT. It can be used with fiber streams that contain a fairly high level of moisture typically greater than 50% on a wt/wt basis.
  • Fiber feedstocks may include, for example, but are not limited to, corn stover, corn gluten feed, distillers' dried grains (DDG), distillers' dried grains with solubles (DDGS), switchgrass, soyhulls, wheat chaff, and wheat straw, palm fiber, bermuda grass, miscanthus and babassu.
  • Fiber feedstocks do not necessarily need to be byproducts of any particular process to obtain some benefit from treatment according to embodiments presented herein. Fiber feedstocks may be pretreated chemically, thermally, and/or mechanically. More detail on fiber feedstocks, particularly corn fiber feedstocks, is found in U.S. Patent Application Publication No. 20060216396A1, to Abbas, et al., entitled "Corn Fiber Hulls as a Food Additive or Animal Feed," which is incorporated by reference herein.
  • Fiber feedstocks often benefit from further processing to produce more useful commodities, such as more readily digestible feed products, biofuel precursors, or industrial chemicals. Because typical byproducts are largely comprised of plant cell walls made of cellulose, hemicellulose, lignin, and proteins, their treatment typically includes enzymatic and/or thermochemical hydrolysis, which generates carbohydrate monomers and oligomers.
  • the hydrolysis does not include any amylases.
  • Amylases are glycoside hydrolase enzymes that break down starch into glucose molecules. Amylase is usually not necessary because the feedstocks have little or no starch. Alkaline treatment of the fiber feedstock while useful in extracting lignin and to break down ester linkages is not always necessary in a typical embodiment.
  • the fiber feedstocks will either contain no starch prior to the protease treatment, or they will have only a small amount of starch.
  • the starch content of the fiber feedstock, by weight may be less than 10%, less than 5%, less than 4%, less than 3%, less than 2%, less than 1%, or less than 0.5%.
  • a typical process of the invention includes thermochemical hydrolysis of a fiber feedstock. This releases some pentoses from the fiber hemicellulose constituent and loosens the fiber structures, particularly that of any remaining cell wall components. Following thermochemical hydrolysis, the fiber feedstock is treated enzymatically to release glucose and other hexoses, as well as to release pentoses including D-xylose and L-arabinose.
  • a typical enzymatic treatment is conducted using a blend of enzymes including one or more cellulases and one or more hemicellulases, though one skilled in the art will recognize that this blend may be modified depending on the initial content of the fiber feedstock and on the results of the thermochemical hydrolysis.
  • an enzymatic treatment includes one or more proteases.
  • the proteases degrade primarily the structural proteins that are cross-liked to other components of the fiber feedstock.
  • the carbohydrate polymers are linked predominantly via N or O type linkages to the amino acids: asparagine, glutamine, serine, hydroxyproline or threonine that are present in the polypeptide backbone. This increases the amount of glucose and other hexoses that are released during the enzymatic treatment. This also reduces the amount of cellulase necessary in a typical hydrolysis.
  • cellulase or “cellulase blend” include one enzyme or a mixture of enzymes that degrade cellulose.
  • Typical cellulases include endocellulase or endoglucanase, exocellulase, exocello-biohydrolase, and cellobiase.
  • Hemicellulase or “hemicellulase blend” include one enzyme or a mixture of enzymes that hydrolyze hemicellulose.
  • Typical hemicellulases include but are not limited to ⁇ -xylanases, ⁇ -arabinofuranosidases, ferulic and acetyl esterases , ⁇ & ⁇ -mannases, ⁇ & ⁇ -galactosidases, and ⁇ - galactomannanases.
  • the effective amount of cellulase, hemicellulase, and protease used in embodiments of the invention will vary with the type of enzymes used in the process, the ultrastructure and composition of the cell wall (which varies by plant type), the pretreatment or pre-processing step, and well as the as the desired yield. Commercial enzymes may be used according to their manufacturer's instructions.
  • Typical proteases for use in the invention include, for example, the aspartic protease from Aspergillus saitoi having the amino acid sequence give in SEQ ID NO:1.
  • Other proteases having at least 50% or greater sequence identity with SEQ ID NO:1 may also be used, so long as the protease activity is conserved.
  • Proteases suitable for use in embodiments of the invention may have a sequence identity with SEQ ID NO: 1 of greater than 50%, greater than 60%, greater than 70%, greater than 80%, greater than 90%, greater than 95%, or greater than 98%, so long as protease activity is retained.
  • proteases include but are not limited to those given in Table 1.
  • the Aspergillus saitoi protease protein sequence was used to blast the NCBI sequence collection and identify proteases with 47% or higher sequence identity.
  • the T. reesei protease was not identified because of too many gaps between the two protease sequences.
  • Sequence identity percentages are based on percentage identity with SEQ ID NO:1. Sequence identity percentages were determined by BLAST in the CGC Wisconsin Genetics Software Packages, Version 10 (available from Accelrys Inc., 9685 Scranton Road, San Diego, Calif., USA). Alignments using BLAST programs can be performed using the default parameters.
  • reaction conditions for hydrolysis including protease need not vary from those typically used for hydrolysis using cellulases or hemicellulases without proteases.
  • reaction temperatures may be, for example, but are not limited to between 25 to 8O 0 C, 40 to 7O 0 C or 50 to 6O 0 C.
  • Reaction times may be, for example, but are not limited to between 30 minutes to 48 hours, typically between 60 minutes and 24 hours.
  • Reaction pH may be, for example, from 2.0 to 7.0, more typically from 4.0 to 5.5. Based on results obtained earlier and present knowledge of acid proteases, some of the reactions may proceed at lower pH ( ⁇ 5.0) and at higher temperature (>55 C). With different fiber materials, the optimum enzyme performance may occur over a wide range of temperature and pH.
  • Example 1 shows hydrolysis of various fiber feedstocks with and without a protease. Percentages are caluculated on a V/V basis.
  • 0.2% cellulase mix including 0.2% GC-220, a Genencor cellulase blend; 0.2% Celluclast L, a Novozymes cellulase blend,
  • Fiber feedstocks were prepared by grinding with a Wiley mill and sieving through a 40 mesh screen. Fiber feedstocks used in the experiment were corn fiber, corn stover, corn gluten feed, distillers' dried grains, distillers' dried grains with solubles, switchgrass, soyhulls, wheat chaff, and wheat straw.
  • Patents, patent applications, publications, scientific articles, books, web sites, and other documents and materials referenced or mentioned herein are indicative of the levels of skill of those skilled in the art to which the inventions pertain, as of the date each publication was written, and all are incorporated by reference as if fully rewritten herein. Inclusion of a document in this specification is not an admission that the document represents prior invention or is prior art for any purpose.

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

L'invention concerne de nouveaux procédés de traitement de fibres et les produits obtenus à partir de ceux-ci. Les procédés peuvent comprendre une hydrolyse thermochimique et/ou enzymatique de matières premières fibreuses, y compris des drêches de distillerie, des drêches de distillerie contenant des matières solubles, des cosses de soja, du miscanthus et du panic raide. L'hydrolyse enzymatique comprend une hydrolyse avec de la cellulase, de l'hémicellulase et de la protéase.
PCT/US2008/079152 2007-10-12 2008-10-08 Hydrolyse de fibres augmentée par addition de protéase WO2009048917A2 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP08836912.9A EP2201127B1 (fr) 2007-10-12 2008-10-08 Hydrolyse de fibres augmentée par addition de protéase
CA2702279A CA2702279C (fr) 2007-10-12 2008-10-08 Hydrolyse de fibres augmentee par addition de protease
BRPI0816621A BRPI0816621A2 (pt) 2007-10-12 2008-10-08 "método para aumentar a quantidade de glicose e outros açúcares e peptídeos liberados de um material de partida de fibra e método para a obtenção de um fibra hidrolisada sólida para a produção de bio-óleo"
ES08836912.9T ES2538995T3 (es) 2007-10-12 2008-10-08 Aumento de la hidrólisis de fibras por adición de proteasa

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US99881807P 2007-10-12 2007-10-12
US60/998,818 2007-10-12

Publications (2)

Publication Number Publication Date
WO2009048917A2 true WO2009048917A2 (fr) 2009-04-16
WO2009048917A3 WO2009048917A3 (fr) 2010-01-21

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PCT/US2008/079152 WO2009048917A2 (fr) 2007-10-12 2008-10-08 Hydrolyse de fibres augmentée par addition de protéase

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US (1) US8815571B2 (fr)
EP (1) EP2201127B1 (fr)
BR (1) BRPI0816621A2 (fr)
CA (1) CA2702279C (fr)
ES (1) ES2538995T3 (fr)
HU (1) HUE025534T2 (fr)
WO (1) WO2009048917A2 (fr)

Families Citing this family (7)

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Publication number Priority date Publication date Assignee Title
DK2958437T3 (da) * 2013-02-21 2020-03-30 Direvo Ind Biotechnology Gmbh Præbiotiske dyrefoderprodukter
US20150189900A1 (en) * 2014-01-07 2015-07-09 Ian Mackay Process for Producing Protein Concentrate or Isolate and Cellulosic Thermochemical Feedstock From Distillers Grains
WO2015120036A1 (fr) * 2014-02-04 2015-08-13 University Of Virginia Patent Foundation Compositions et procédés pour l'analyse de séquences de protéines et de modifications post-traductionnelles
RU2019102378A (ru) 2016-06-30 2020-07-30 ДАНИСКО ЮЭс ИНК. Аспарагиновые протеазы
CN107384899B (zh) * 2017-08-01 2020-03-27 中国农业科学院饲料研究所 一种真菌来源的酸性蛋白酶g412及其基因和应用
CN110226667B (zh) * 2019-06-11 2022-08-09 翔宇药业股份有限公司 一种处理复方红衣补血口服液药渣的环保工艺
EP4221517A1 (fr) * 2020-10-02 2023-08-09 Hamlet Protein A/S Ingrédient d'aliment pour animaux ou d'aliment dérivé de biomasse de coques de soja riche en fibres

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4737365A (en) * 1986-01-13 1988-04-12 Central Soya Company, Inc. Method of feeding cattle to improve protein utilization
JP3321626B2 (ja) * 1993-07-19 2002-09-03 株式会社はくばく 炊飯時の食感が改良された大麦の製造方法
US7005128B1 (en) * 1993-12-17 2006-02-28 Genencor International, Inc. Enzyme feed additive and animal feed including it
GB9416841D0 (en) * 1994-08-19 1994-10-12 Finnfeeds Int Ltd An enzyme feed additive and animal feed including it
EP1320588B2 (fr) * 2000-09-25 2017-06-28 Iogen Energy Corporation Procede de production de glucose a partir d'un melange comprenant une cellulase modifiee
US6506423B2 (en) * 2000-12-21 2003-01-14 Kansas State University Research Foundation Method of manufacturing a ruminant feedstuff with reduced ruminal protein degradability
DE60238339D1 (de) * 2001-08-27 2010-12-30 Syngenta Participations Ag Selbstprozessierende pflanzen und pflanzenteile
US20040023349A1 (en) * 2002-06-13 2004-02-05 Novozymes A/S Processes for making ethanol
MXPA05009315A (es) * 2003-03-07 2005-11-08 Ca Minister Agriculture & Food Uso de enzimas proteoliticas para aumentar la utilizacion de pienso en las dietas de rumiantes.
ATE530643T1 (de) * 2004-12-30 2011-11-15 Genencor Int Säureaktive fungale protease
CN101160405B (zh) * 2005-04-12 2014-01-01 纳幕尔杜邦公司 处理生物质以获得目标化学物质
CA2605125C (fr) * 2005-04-19 2012-04-17 Archer-Daniels-Midland Company Procede pour la production d'aliment pour animaux et d'ethanol et aliment nouveau
WO2006138005A2 (fr) * 2005-05-10 2006-12-28 Monsanto Technology, Llc Genes et leurs utilisations pour l'ameliorations de plantes

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
SINGH ET AL.: "Modified Dry Grind Ethanol Process", AG. ENG. DEPT., 18 July 2001 (2001-07-18)

Also Published As

Publication number Publication date
EP2201127B1 (fr) 2015-03-18
US8815571B2 (en) 2014-08-26
CA2702279A1 (fr) 2009-04-16
EP2201127A2 (fr) 2010-06-30
WO2009048917A3 (fr) 2010-01-21
BRPI0816621A2 (pt) 2016-08-30
EP2201127A4 (fr) 2012-05-16
US20090098638A1 (en) 2009-04-16
HUE025534T2 (en) 2016-04-28
ES2538995T3 (es) 2015-06-25
CA2702279C (fr) 2017-02-14

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